EGFR c.956A>G ;(p.E319G)

Variant ID: 7-55223589-A-G

NM_005228.3(EGFR):c.956A>G;(p.E319G)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Oncogene Mutation Survey in MPNST Cell Lines Enhances the Dominant Role of Hyperactive Ras in NF1 Associated Pro-Survival and Malignancy.

Translational Oncogenomics
Sun, Daochun D; Tainsky, Michael A MA; Haddad, Ramsi R
Publication Date: 2012

Variant appearance in text: EGFR: E319G
PubMed Link: 22346343
Variant Present in the following documents:
  • Main text
  • tog-5-2012-001.pdf
View BVdb publication page